Schneider Birgit, Junge Friederike, Shirokov Vladimir A, Durst Florian, Schwarz Daniel, Dötsch Volker, Bernhard Frank
Centre for Biomolecular Magnetic Resonance, University of Frankfurt/Main, Institute for Biophysical Chemistry, Frankfurt/Main, Germany.
Methods Mol Biol. 2010;601:165-86. doi: 10.1007/978-1-60761-344-2_11.
Cell-free expression has emerged as a promising tool for the fast and efficient production of membrane proteins. The rapidly growing number of successfully produced targets in combination with the continuous development of new applications significantly promotes the distribution of this technology. Membrane protein synthesis by cell-free expression does not appear to be restricted by origin, size or topology of the target, and its global application is therefore a highly valuable characteristic. The technology is relatively fast to establish in standard biochemical labs, and it does not require expensive equipment. Moreover, it enables the production of membrane proteins in completely new modes, like the direct translation into detergent micelles, which is not possible with any other expression system. In this protocol, we focus on the currently most efficient cell-free expression system for membrane proteins based on Escherichia coli extracts.
无细胞表达已成为一种用于快速高效生产膜蛋白的有前景的工具。成功生产的靶标数量迅速增加,再加上新应用的不断开发,极大地推动了这项技术的推广。通过无细胞表达合成膜蛋白似乎不受靶标的来源、大小或拓扑结构的限制,因此其广泛适用性是一项非常有价值的特性。该技术在标准生化实验室中相对容易建立,并且不需要昂贵的设备。此外,它能够以全新的模式生产膜蛋白,例如直接翻译到去污剂胶束中,这是任何其他表达系统都无法实现的。在本方案中,我们重点介绍基于大肠杆菌提取物的目前最有效的膜蛋白无细胞表达系统。